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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762300Generated: October 26, 2026

Triethylamine → N-cyclopropyl-3-trifluoromethylbenzylsulfonamide

https://huagongshe.com/reaction/1762300

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantCyclopropylamineHCID 69828—
Reactant3-(Trifluoromethyl)phenylmethanesulfonyl chlorideHCID 2794646—
SolventDichloromethaneHCID 6344—
ProductN-cyclopropyl-3-trifluoromethylbenzylsulfonamideHCID 1561599492.6%

Reaction Steps

In this example 5.3 g of cyclopropylamine were mixed with 9.4 g of triethylamine and then added drop-wise to a solution containing 20 g of 3-trifluoromethylbenzylsulfonyl chloride in methylene chloride at 0° C. The resulting reaction mixture was stirred at room temperature (i.e., about 20°-25° C.) for 3 hours. The reaction mixture was then washed with saturated aqueous ammonium chloride and then with aqueous 1 wt. % hydrochloric acid until it was neutral. The organic layer was then separated, washed twice with 50 ml of aqueous saturated sodium chloride solution, dried over magnesium sulfate and then evaporated to dryness affording 20 g of N-cyclopropyl-3-trifluoromethylbenzylsulfonamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04831179
Source datasetuspto-grants-1989_05
ORD IDord-e9d694cef89f439f969bfdde7f6e6345
Source noteuspto-grants-1989_05